[Remote] Clinical Research Associate (CRA I, II, Sr)
Note: The job is a remote job and is open to candidates in USA. Theradex Oncology is a leader in cancer therapy development, seeking Clinical Research Associates to support oncology studies. The role involves site monitoring, source document verification, and ensuring ethical conduct of clinical trials.
Responsibilities
⢠Onsite and remote monitoring of phase I-III oncology studies
⢠Responsible for all aspects of site monitoring
⢠Source document verification and site management
⢠Monitoring oncology studies
⢠Communicate effectively with sponsors and site staff
Skills
⢠At minimum, Bachelor's degree in biological or science-related field (BSc, BA, or RN equivalent) or equivalent
⢠Clinical Research Associate experience managing clinical trial sites. The number years and type of monitoring experience will determine the level to which you'll be considered
⢠Knowledge of ICH-GCP guidelines and applicable regulatory requirements
⢠Exceptional communication, interpersonal, and problem-solving skills
⢠Proficiency in Microsoft Office Suite
⢠Strong attention to detail, organization, and time management abilities
⢠Willingness to travel up to 50% may involve overnight stays
⢠Successfully pass background clearance checks which may be run on a periodic basis due to 3rd party contractual obligation requirements
⢠English fluency (written and verbal)
⢠Experience in monitoring oncology studies is preferred for CRAI and CRAII
⢠Sr CRAs must have proven experience independently monitoring oncology phase I-III studies
⢠Valid Driver's License and Passport preferred
Benefits
⢠Medical, dental and vision coverage
⢠Life insurance
⢠Disability insurance (STD/LTD)
⢠Company matched 401(k)
⢠Very competitive tuition reimbursement
⢠Generous vacation/sick plans
⢠Flexible work schedules
⢠Employee discounts
⢠Other company provided benefits
Company Overview
⢠Theradex Oncology, your full-service CRO for all indications and modalities. It was founded in 1982, and is headquartered in Princeton, New Jersey, USA, with a workforce of 51-200 employees. Its website is http://theradex.com.
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Responsibilities
⢠Onsite and remote monitoring of phase I-III oncology studies
⢠Responsible for all aspects of site monitoring
⢠Source document verification and site management
⢠Monitoring oncology studies
⢠Communicate effectively with sponsors and site staff
Skills
⢠At minimum, Bachelor's degree in biological or science-related field (BSc, BA, or RN equivalent) or equivalent
⢠Clinical Research Associate experience managing clinical trial sites. The number years and type of monitoring experience will determine the level to which you'll be considered
⢠Knowledge of ICH-GCP guidelines and applicable regulatory requirements
⢠Exceptional communication, interpersonal, and problem-solving skills
⢠Proficiency in Microsoft Office Suite
⢠Strong attention to detail, organization, and time management abilities
⢠Willingness to travel up to 50% may involve overnight stays
⢠Successfully pass background clearance checks which may be run on a periodic basis due to 3rd party contractual obligation requirements
⢠English fluency (written and verbal)
⢠Experience in monitoring oncology studies is preferred for CRAI and CRAII
⢠Sr CRAs must have proven experience independently monitoring oncology phase I-III studies
⢠Valid Driver's License and Passport preferred
Benefits
⢠Medical, dental and vision coverage
⢠Life insurance
⢠Disability insurance (STD/LTD)
⢠Company matched 401(k)
⢠Very competitive tuition reimbursement
⢠Generous vacation/sick plans
⢠Flexible work schedules
⢠Employee discounts
⢠Other company provided benefits
Company Overview
⢠Theradex Oncology, your full-service CRO for all indications and modalities. It was founded in 1982, and is headquartered in Princeton, New Jersey, USA, with a workforce of 51-200 employees. Its website is http://theradex.com.
Apply tot his job
Apply To this Job